Variant report
| Variant | rs992998 |
|---|---|
| Chromosome Location | chr6:71820001-71820002 |
| allele | A/C |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr6:71817800-71823400 | Weak transcription | Primary monocytes fromperipheralblood | blood |
| 2 | chr6:71817800-71824400 | Weak transcription | HUES64 Cell Line | embryonic stem cell |
| 3 | chr6:71818000-71821200 | Weak transcription | H9 Derived Neuron Cultured Cells | ES cell derived |
| 4 | chr6:71818000-71824200 | Weak transcription | Ganglion Eminence derived primary cultured neurospheres | brain |
| 5 | chr6:71818200-71824200 | Weak transcription | Primary neutrophils fromperipheralblood | blood |
| 6 | chr6:71818600-71823200 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
| 7 | chr6:71818800-71820600 | Weak transcription | H1 Derived Mesenchymal Stem Cells | ES cell derived |
| 8 | chr6:71818800-71821000 | Weak transcription | NH-A | brain |
